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首页> 外文期刊>Angiology: the Journal of Vascular Diseases >Polymorphisms of renin-angiotensin system and natriuretic peptide receptor A genes in patients of Greek origin with a history of myocardial infarction.
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Polymorphisms of renin-angiotensin system and natriuretic peptide receptor A genes in patients of Greek origin with a history of myocardial infarction.

机译:患有心肌梗塞病史的希腊裔患者的肾素-血管紧张素系统和利钠肽受体A基因多态性。

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摘要

We assessed the association between (CA)n repeat polymorphism of angiotensinogen (AGT), 250 base pair (bp) insertion/deletion (I/D) of angiotensin-converting enzyme (ACE), tetranucleotide repeat polymorphism (TCTG)n of renin (REN), (CT)n repeat polymorphism of the natriuretic peptide receptor A (NPRA) genes, and the presence and extent of coronary artery disease (CAD) in Greek patients with a history of myocardial infarction (MI). A total of 158 post-MI patients referred for coronary angiography were compared with 144 controls. The SS genotype of the AGT gene was related with an increased risk for 3-vessel CAD (odds ratio [OR], 1.94; 95% confidence interval [CI], 1.05-3.61; P = .041), whereas the SL genotype was related with a decreased risk (OR, 0.44; 95% CI, 0.22-0.87; P = .019). Moreover, there was a trend for the SL genotype of the REN gene toward increased risk for CAD. There was a significant association between (CA)n polymorphism of the AGT gene and the extent of CAD in Greek patients with a history of MI.
机译:我们评估了血管紧张素原(AGT)的(CA)n重复多态性,血管紧张素转化酶(ACE)的250个碱基对(bp)插入/缺失(I / D),肾素的四核苷酸重复多态性(TCTG)n之间的关联( REN),(CT)n在希腊有心肌梗塞(MI)史的患者中,利钠肽受体A(NPRA)基因的重复多态性以及冠状动脉疾病(CAD)的存在和程度。将总共​​158例接受MI术后冠状动脉造影的患者与144例对照进行了比较。 AGT基因的SS基因型与增加3血管CAD的风险有关(比值比[OR]为1.94; 95%置信区间[CI]为1.05-3.61; P = .041),而SL基因型为与降低的风险相关(OR为0.44; 95%CI为0.22-0.87; P = 0.019)。此外,REN基因的SL基因型有增加CAD风险的趋势。在有MI史的希腊患者中,AGT基因的(CA)n多态性与CAD的程度之间存在显着关联。

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